NDC 69267-101 Atenolol Scopolamine

  1. Labeler Index
  2. Tps
  3. NDC Product Code: 69267-101 Atenolol Scopolamine

Product Information

Product Code69267-101
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Atenolol Scopolamine
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Tps
Labeler Code69267
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		10-01-2014
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.		12-31-2017
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I". 		I
NDC Code Structure

Product Characteristics

Color(s)WHITE (C48325)
ShapeROUND (C48348)
Size(s)5 MM
Score1

Product Packages

NDC 69267-101-06

Package Description: 151.5 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-12

Package Description: 303 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-24

Package Description: 606 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-48

Package Description: 1212 mg in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Atenolol Scopolamine is product labeled by Tps. The product's dosage form is and is administered via form.


What are Atenolol Scopolamine Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ATENOLOL (UNII: 50VV3VW0TI)
  • ATENOLOL (UNII: 50VV3VW0TI) (Active Moiety)
  • SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
  • SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)


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Atenolol Scopolamine Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

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